lithium bis(trimethylsilyl)azanide

CN1CCN(c2ccc(O)cc2)CC1
Reaction #339
Ausbeute 51.0%750 AstraZeneca ELN dataset
COc1cccc(N2CCC(C#N)CC2)c1
Reaction #391
Ausbeute 28.5%750 AstraZeneca ELN dataset
COc1cccc(N2CCC(C#N)CC2)c1
Reaction #392
Ausbeute 54.5%750 AstraZeneca ELN dataset
COc1cccc(N2CCC(C(N)=O)CC2)c1
Reaction #393
Ausbeute 0.0%750 AstraZeneca ELN dataset
c1cc2cn[nH]c2cc1N1CCCC1
Reaction #648
Ausbeute 93.7%750 AstraZeneca ELN dataset
OC1CCN(c2ccncc2)C1
Reaction #651
Ausbeute 43.0%750 AstraZeneca ELN dataset
NC(=O)CCNc1ccc(C(=O)O)cc1
Reaction #686
Ausbeute 0.0%750 AstraZeneca ELN dataset
CCOC(=O)CN1C(=O)[C@@H](NC(=O)OC(C)(C)C)CCC[C@H]1C
Reaction #1295
title product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCOC(=O)CN1C(=O)[C@@H](NC(=O)OC(C)(C)C)CCC[C@H]1C
Reaction #1431
title product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=C1C2CCN(C2)C1C(O)(c1ccccc1)c1ccccc1
Reaction #5072
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
CCC(=O)CN([C@H]1CCN([C@@H](C)C(=O)OC(C)(C)C)C1=O)S(=O)(=O)c1ccc2cc(Cl)ccc2c1
Reaction #7374
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
C[C@@H](C(=O)OC(C)(C)C)N1CC[C@H](N(C)S(=O)(=O)c2ccc3cc(Cl)ccc3c2)C1=O
Reaction #7376
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
C[C@@H](C(=O)N1CCOCC1)N1CC[C@H](N(CC#N)S(=O)(=O)c2ccc3cc(Cl)ccc3c2)C1=O
Reaction #7404
title compound
Ausbeute 27.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
C[C@@H](C(=O)N1CCCCC1)N1CC[C@H](N(CC#N)S(=O)(=O)c2ccc3cc(Cl)ccc3c2)C1=O
Reaction #7411
title compound
Ausbeute 43.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CCOC(=O)C1CC2(CCC1=O)OCCO2
Reaction #7773
8-oxo-1,4-dioxa-spiro[4.5]decane-7-carboxylic acid ethyl ester
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
O=C(Cc1cccc(Cl)n1)c1ccc(F)cc1
Reaction #8584
2-(6-chloro-2-pyridinyl)-1-(4-fluorophenyl)ethanone
Ausbeute 66.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
COc1ccc(C(=O)Cc2cccc(Cl)n2)cc1
Reaction #8593
2-(6-chloro-2-pyridinyl)-1-(4-methoxyphenyl)ethanone
Ausbeute 86.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
O=C(Cc1cc(Cl)ccn1)c1ccc(F)cc1
Reaction #8600
2-(4-chloro-2-pyridinyl)-1-(4-fluorophenyl)ethanone
Ausbeute 99.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CC(C)(C)OC(=O)N1CCC(CCO[Si](C)(C)C(C)(C)C)(C(=O)CC(O)Cc2ccccc2)CC1
Reaction #8867
tert-Butyl 4-(4-phenyl-3-hydroxy-1-oxobut-1-yl)-4-(2-(tert-butyldimethylsilyloxy)eth-1-yl)piperidine-1-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CCOC(=O)c1oc2nc(-c3ccc(Cl)cc3Cl)c(-c3ccc(Cl)cc3)cc2c1N
Reaction #8882
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
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